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Reprocessed SoundStar 3D Diagnostic Ultrasound Catheter

Page Type
Cleared 510(K)
510(k) Number
K170474
510(k) Type
Traditional
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2017
Days to Decision
120 days
Submission Type
Summary

Reprocessed SoundStar 3D Diagnostic Ultrasound Catheter

Page Type
Cleared 510(K)
510(k) Number
K170474
510(k) Type
Traditional
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2017
Days to Decision
120 days
Submission Type
Summary